Philips DigitalDiagnost

C50 High Performance

room

712201

Site preparation specifications

GENERIC

Project reference Typical DigitalDiagnost C50 HP TH

Document date 14-02-2019

Philips contact

Telephone

e-mail
Important information
Important!
This package provides only indicative information intended for use in very early project phases to
provide an impression of room set ups and required site preparation. Any information, figure or value
shown is not necessarily applicable, accurate and/or up-to-date. Your Philips contact can arrange
Room Designs and Site preparation specifications for your specific situation.

Important information Page 1 of 1

Table of contents
1 General ................................................................................................................................................................................2
1.1 Purpose ............................................................................................................................................................................................................................................. 2
1.2 Roles ...................................................................................................................................................................................................................................2
1.3 Conditions of use .........................................................................................................................................................................................................2
1.4 Responsibilities...............................................................................................................................................................................................................................2
1.5 Site readiness ................................................................................................................................................................................................................. 3
1.6 Health & Safety ............................................................................................................................................................................................................. 3
1.7 Equipment details .......................................................................................................................................... 4
2 Building ........................................................................................................................................................................................... 8.
2.1 General information ................................................................................................................................................................................................... 8
2.2 Floor requirements / Floor provisions ............................................................................................................................................................. 8
2.3 Ceiling requirements / Ceiling provisions .......................................................................................................................................................9
2.4 Wall requirements / Wall provisions .............................................................................................................................................................10
3 Electrical ............................................................................................................................................................................11
3.1 General information .................................................................................................................................... 12
3.2 Power ................................................................................................................................................................. 12
3.3 Ducting specifications ............................................................................................................................................................................................. 14
3.4 Networking specifications.................................................................................................................................................................................... 15
4 Mechanical ........................................................................................................................................................... 16
4.1 General information ..................................................................................................................................... 16
4.2 Heating, Ventilation & Air Conditioning (HVAC) ........................................................................................... 16
4.3 Liquid cooling ...............................................................................................................................................16
4.4 Water ................................................................................................................................................................. 16
4.5 Sewerage............................................................................................................................................................. 17
4.6 Sprinkler. ............................................................................................................................................................. 17
4.7 Compressed air ......................................................................................................................................................... 17
4.8 Gases................................................................................................................................................................... 17
5 Environmental protection ........................................................................................................................... 18
5.1 X-ray ................................................................................................................................................................... 18
6 Drawings ............................................................................................................................................................ 19
6.1 Site specific drawings. .................................................................................................................................... 19
7 Annex .................................................................................................................................................................. 20
7.1 Electrical diagram .......................................................................................................................................... 20

Table of contents Page 1 of 21

1 General

1.1 Purpose
The Site preparation specifications should provide all required information to the customer and relevant
contractors to enable the site to be prepared to the necessary quality and timescales ready for delivery and
installation of the equipment.

1.2 Roles
Within this document the following groups are referred to:
• Philips: Equipment manufacturer, equipment supplier
• Customer: Purchaser, end user
• Contractor / Third party: member of the Architect, Engineers & Contractors (AEC) community, hired
by either the customer or Philips

1.3 Conditions of use

The information within this document and any included drawings is provided solely for the purpose of
providing the customer and/or their architects/building contractors, or the Philips appointed building
contractor, with information concerning the Philips equipment locations and associated details, e.g. fixing
positions, cable duct routes etc.
This document and any included drawings are not for architectural or building construction purposes other
than stated above.
The enabling works detailed in this manual is solely for the installation of Philips supplied equipment, any
additional requirements by the customer must be clearly identified and notified to Philips Healthcare and
are the responsibility of the customer.
Philips assumes no liability nor offers any warranty for the fitness or adequacy of the premises or the utilities
available at the premises in which the equipment is to be installed, used, or stored.
All work described must be carried out in compliance with specifications indicated in this package provided
by Philips Healthcare; any deviation must first be agreed by Philips Healthcare project manager.
The specifications laid out in this document can be subject to change by Philips. All parties must ensure they
are using the latest version.

1.4 Responsibilities
The customer is responsible for any classification of the room in relation to its intended use, and must notify
Philips Healthcare project manager and the contractors of any additional specifications this may include.
The customer remains responsible for all works that are necessary for site preparation, unless works that
are included in the Philips contract, in which case the term "customer" can be read as "Philips contractor".
The customer should ensure that the work areas are lockable with limited access. Philips Healthcare should
have access to the areas (via keys / access codes) prior to the start and during the installation.
The customer shall advise Philips of conditions at or near the site which could adversely affect the carrying
out of the installation work and shall ensure that such conditions are corrected and that the site is fully
prepared and available to Philips before the installation work is due to begin.
The contractor and or architect must ensure that the works carried out in line with this document comply
with local regulations unless more strict requirements are set out by this document or defined by the
customer.

General Page 2 of 21
1.5 Site readiness
We expect the site of the installation to be completely finished, clean, dry, and clear of contractors and
meet the requirements defined in this document before the equipment delivery / start of the installation.
Failure to meet these requirements could result in delays to the timelines, additional charges etc.

1.6 Health & Safety

1.6.1 Radiation considerations for ionizing radiation (X-ray, gamma ray)
The equipment specified in this document uses ionizing radiation (e.g. X-ray, gamma ray) for diagnostic
imaging, therefore safety measures have to be applied to avoid hazards to patients, visitors and staff. It is
the customer's responsibility to comply with local regulation and to ensure:
• The size, position, angle of vision and radiation protection capabilities of protective shielding & the
effectiveness of other radiation protection, radiation warning devices, and further equipment is
approved by the local radiation protection authority.
• The required radiation protection is in place at the start of the installation as test images have to
be made during the installation.
• That there is sufficient protection from any other existing external sources of ionizing radiation for the
Philips employees and representatives during the installation process.
• When drilling holes in protective screen, walls, floor and ceiling it must be ensured that the radiation
integrity of the room is maintained.
Equipment data to support the protection calculations by the local radiation protection authority are listed
in section Environmental protection of this document.

Note!
Equivalents for lead (1 mm Pb)
There are other materials which can be used for protection as an alternative to lead (however this
must be specified by the local radiation protection authority)
• 8 cm concrete: 2.2 g/cm3
• 11 cm brick: 1.6 g/cm3

General Page 3 of 21
1.7 Equipment details
1.7.1 Equipment and delivery specifications
The table lists the basic specifications for the ordered equipment.

Rails and longitudinal carriage (CSV2 Standard - Comfort Track)

IC N - 1503- 746- GG -01- 11-

Width (W) Depth (D) Height (H) Weight Notes

[mm] [mm] [mm] [kg]
Ceiling ra ils + longitudinal carriage (A)
Packed 3854 1054 350 2150 Weight incl. longitudinal carriage
Installed 3720 2900 209 140 Incl. standard ceiling rails

Transvers al carriage (B)

Packed 1414 1054 1660 360 Telescopic carriage (a) incl. tube
assembly (b)
Installed 650 1060 916 (min) 180
2990 (max)

Patient table (DiDi TH)

a
IC N - 1403- 712- GG -01- 01-A

W D

Width (W) Depth (D) Height (H) Weight Notes

[mm] [mm] [mm] [kg]
Table base (a)

Packed 1400 1010 890 310 Crate

Transport 1350 960 830 250 Foil
Table top (b)
Transport 2500 890 240 82 750 mm
Installed 2400 750 915 251 Assembled table base and table top

General Page 4 of 21
Vertical stand 2 (VS2) tilted

Width (W) Depth (D) Height (H) Weight Notes

[mm] [mm] [mm] [kg]

Packed 2220 760 550 170 Column (a)

Packed 1030 970 900 150 Vertical tilting unit (b)
Installed 902 986 2085 255 Stand

Other equipment
Width (W) Depth (D) Height (H) Weight Notes
[mm] [mm] [mm] [kg]
Generator (M-cabinet CXA Pro)
Packed 631 843 1274 205 Generator
Packed 495 140 1000 34 Wall box
Installed 702 488 980 136 Generator
Installed 488 135 1900 20 Wall box

Operator' s console
Packed 630 565 370 17.5 Eleva Examination Control A
Packed 555 465 358 16.0 AWS-TX
Installed 529 207 359 8.4 Eleva Examination Control A
Installed 215 276 449 14.1 AWS-TX
Varian (PaxScan) detector
Packed - - - - -
Installed 460 16 385 3.6 Varian Detector
Installed 220 160 34 1.0 Varian Battery charger
Installed 175 205 65 1.1 Wireless access point

General Page 5 of 21
 Delivery details
The delivery routes will be checked in advance by the Philips Healthcare project manager.
Requirement
The table lists the critical requirements for delivery. In case of any potential problems with these
requirements please contact Philips Healthcare project manager.
Requirement Specification

Site accessibility Large truck, forklift and in special cases a crane.

Minimum door height ≥ 1700 mm (excl. protective floor covering)
Minimum door width ≥ 970 mm
Minimum corridor width ≥ 1070 mm
(including 100mm margin for wall mounted obstacles)
Corridor widths (X&Y) at a 90° bend Y ≥ 2785 mm
(see illustration) when X= minimum door width (Y can be smaller when
X is wider)

Minimum elevator cage size 2750x1050x1500 mm

(WxDxH) (longest packages via an alternate route)
Elevator & floor loading The equipment delivery route must be suitable to take
the load and delivery of the packages and the transport
tools (e.g. pallet truck, dolly, etc.)

A
Y
IC N - V -1403- 000-GG-01- 01-A

Transportroute/ Corridor widths(X& Y)and door opening(A)

1.7.2 Storage conditions
If storage of the equipment at the customer site is required and agreed with the Philips Healthcare project
manager, the following critical requirements must be maintained. In case of any potential problems with
these requirements please contact the Philips Healthcare project manager.
Requirement Specification

Temperature -10 to +70 °C

Humidity 10 - 95%, non-condensing
Vibration -

1.7.3 Equipment noise levels

The table lists the basic specifications for the ordered equipment.

General Page 6 of 21
Equipment Noise level [d B(A)]

(operational) (standby)
Ceiling suspension (CSV2) ≤ 55 ≤ 55
with longitudinal carriage
Patient table (DiDi TH 750mm) - -
Vertical stand 2 (VS2) ≤ 55 ≤ 55
X-ray generator (M-cabinet CXA Pro) < 52 -
(at 1 m distance 1 m above
floor)

Eleva Workspot (AWS-TX + EEC-A) ≤ 43 -

General Page 7 of 21
2 Building

2.1 General information

Please ensure that you read all sections of this document and take care to work with the other contractors
on any overlapping activity.
All work described must be carried out in compliance with specifications indicated in this package provided
by Philips Healthcare. Any deviations must first be agreed by Philips Healthcare project manager.
All work described in this section is to be executed and supplied by the relevant contractor / party, unless
otherwise indicated as Philips Healthcare, or defined in a subsequent document.
The area must be prepared to accept cable ducting as required (Feed-through & troughs).
When drilling holes and Feed-throughs in the walls, floor and ceiling it must be ensured that the structural
integrity of the room is maintained.
The contractor must ensure that fixing holes, especially tapped holes, are kept clear of any paint / levelling
compound etc.
The contractor must ensure that the reference axes, as shown on the drawings, are precisely aligned, and
marked on the floor (and ceiling when ceiling provisions are applicable).

2.2 Floor requirements / Floor provisions

Floor levelness and waviness
Floor levelness and waviness are critical for the correct operation of the system and will be checked in
advance of the installation.
Refer to the chapter Drawings , sheet Floor provisions for more information.
The contractor must ensure that the floor mounting / placement areas defined meet the specifications to
receive the holes, fixings and take the load.
The mounting points on the floor must be suitable for the tensile strengths and sheer forces as indicated in
the table below.
There shall be no obstructions on the floor (sliding door tracks, etc.) in front of the Philips technical
cabinets. Floor must be clear to allow cabinets to be pulled away from the wall for service.
The customer must ensure that the chosen floor covering is fit for purpose and meets the requirements of
any room classifications that may apply.
The contractor must ensure that, if present, any floor ducting should be sealed after the completed
installation to prevent the ingress of fluids.
2.2.1 Floor requirements table
Overview of floor mounted equipment and fixation specifications
Refer to the chapter Drawings , sheet Floor provisions for location, quantities and responsibilities
Equipment Weight [kg] Fixings Forces [N]

Patient table (DiDi TH 750mm) 251 4x M12 safety 3600 (each

bolts screw)
Vertical stand 2 (VS2) wall mounted 255 3x M12 bolts 500 (each bolt)
X-ray generator (M-cabinet CXA Pro 50/65 kW) 136 - -

Building Page 8 of 21
2.2.2 Floor requirements illustrations
Illustration(s)
Refer to the chapter Drawings, sheet Floor provisions for the site specific drawings.

2.3 Ceiling requirements / Ceiling provisions

The support structure surface upon which Philips equipment is to be placed / anchored must:
• Be flat and level to within 1 mm
• Square and parallel in each direction (vertical and horizontal) to within 1 mm
• Withstand the forces of retardation in longitudinal and transversal direction up to 0.45 kN,
max. to 2.6 kN in longitudinal direction.

Ceiling clearance
Lighting fixtures must be placed in such a position that they are not obscured by equipment or its
movement, or interfere with the movement of Philips equipment (e.g. monitor suspensions) or otherwise
adversely affect the equipment.

Keep the underside of the finished ceiling clear of objects:

• For an area of 80 mm outside the range of the carriage clear of objects that protrude more than
120 mm below the ceiling (A);
• For an area of 300 mm around the Philips Ceiling Suspension (CSV) rails clear of ALL objects (B);
• An area of 900 mm is necessary for insertion of the CSV carriage (C).

C
IC N - V -1403- 746-GG- 02-01- A

2.3.1 Ceiling requirements table

Overview of ceiling mounted equipment and fixation specifications
Refer to the chapter Drawings, sheet Ceiling provisions for location, quantities and responsibilities.
Equipment Weight [kg] Fixings Forces [N]
Ceiling suspension (CSV2) 320 (incl. 3720 M10x40 bolts (2 4250 (each
with longitudinal carriage mm rail) bolts/mounting bolts)
point)

Building Page 9 of 21
2.3.2 Ceiling requirements illustrations
Illustration(s)
Refer to the chapter Drawings, sheet Ceiling provisions for the site specific drawings.
ICN-V-1403-000-GG-02-02-A

A B

Typical example of afalse ceiling (A)withceiling support

structure (B)
Description of the support structure
The Philips ceiling rails should be mounted on anchor rails (metal framing). The anchor rails are the
interface for installing the ceiling rails. The following anchor rail system(s) are allowed:
• Unistrut, type P1000 / P1001
• MSR-Profile (similar Wieland-anchor rails)
• Graaf-Profile (similar Wieland-anchor rails)

A complete set of fixing material to mount the Philips equipment to the anchor rails (including isolation /
installation / insulation plates and shims) is part of the delivery. Further details can be seen in the drawings.
If Beam Clamps are used to fix Unistruts/Marstrut to steelwork, a suitable shake proof type must be used.
The load bearing struts are indicated in the drawings. When applicable extra struts/profiles are indicated to
serve as frame work for suspended ceiling tiles.
The contractor must take measures (like tagging) to prevent drilling and/or screwing in the lower metal
framing channels.

2.4 Wall requirements / Wall provisions

The contractor must ensure the walls are flat and perpendicular to the floor.
The contractor must ensure that wall mounting areas defined meet the specifications to receive the holes,
fixings, and take the load.
2.4.1 Wall requirements table
Overview of wall mounted equipment and fixation specifications
Refer to the chapter Drawings, sheet Wall provisions for location, quantities and responsibilities.
Equipment Weight [kg] Fixings Forces [N]
Vertical stand 2 (VS2) wall mounted 255 4x M12 bolts 1500 (each bolt)
Wall box for x-ray generator (M-cabinet CXA Pro 50/65 kW) 20 8x M8 bolts 750

Building Page 10 of 21
2.4.2 Wall requirements illustrations
Illustration(s)
Refer to the chapter Drawings, sheet Wall provisions for the site specific drawings.
IC N - 1403- 742- GG -02- 01-A

Mechanical fixings for generator cabinet

Building Page 11 of 21
3 Electrical

3.1 General information

The contractor must ensure that live power is provided as specified to the areas defined and is switchable
and tested prior to the start of the installation.
The customer must ensure that the mains supply isolator for the equipment in the room must be
conveniently accessible to the contractor.
The cable ducting shown in the drawings should not be used for any cables other than those for the Philips
Healthcare equipment.
The contractor must ensure that at least 1200 mm free cable length is left on each unconnected end for all
contractor-supplied cabling unless otherwise stated

3.2 Power
3.2.1 Power specifications
The power specifications are determined by the X-ray generator which generates high voltage for the X-
ray tube in the equipment.
3.2.2 Power quality
The power supply to the system must meet the following voltage quality and frequency requirements.
Requirement Specification

Voltage 3 x 400 - 480 V +10 %

Frequency 47 - 63 Hz

3.2.3 Power consumption

Requirement Specification

Mains connection Ifuse x U x √3

Maximum power 50/65 kW
Maximum mains current (at 400 V) 112 A / 134 A (50/65 kW)
(at 480 V) 95 A / 115 A (50/65 kW)
Fuse protection (50/65 kW) 35 A / 50 A, slow blow
Mains resistance (at 400 V) (50/65 kW) < 300 mΩ / 200 mΩ
(at 480 V) (50/65 kW) < 400 mΩ / 300 mΩ

3.2.4 Circuit breaker

An earth-leakage circuit breaker is to be provided between the mains fuse and the medical equipment
depending on local regulations.

The earth-leakage circuit breaker meets the following specification:

• Rated fault current: 0.03 A
• Rated current: 63 A
• Type of circuit breaker: A or B
• Connection terminals for wire cross sections of up to 25 mm2

Electrical Page 12 of 21
3.2.5 Earthing
Note!
The earth connection requirements for medical equipment exceed those for ordinary electrical
installations. The contractor must ensure that local regulations are followed closely.

In all situations, the contractor must ensure that there is one (1!) earth reference terminal (ERT) for all
Philips supplied equipment, and it should be connected via a removable link (A) to the customer earth.

A
ERT

Philips
ICN-V-1103-000-GG-03-C

Typicallayout of an EarthReferenceTerminal
3.2.6 Lighting & Small Power
The contractor must ensure that sockets for the Philips equipment only are provided as per the drawings.
3.2.7 Safety mechanism requirements
The Philips system is equiped with several additional safety provisions. The use of these provisions is
regulated by local legislation. Philips Healthcare advises to install the safety provisions at all times to reach
maximum safety for personnel and patient.

B D C

+24 V
+24 V

A
ICN-V-1403-742-GG-03-01-A

230 Vac

Typical diagram for safety mechanism requirements

Electrical Page 13 of 21
 X-ray ON warning lights
For the X-ray on warning light(s) (A), the system is provided with a relay contact in the generator which
can switch a maximal 6 A and can be connected to maximum 230 V as shown in the illustration above.
The contractor must ensure that the lamp provided has a response time between 1 - 1000 msec.
The contractor must ensure that the X-ray on warning lights are mounted as per the drawings and cables
are routed to the X-ray generator. It is allowed to use Philips dedicated cable ducting for this purpose.
The Philips engineer will connect the cables to the X-ray generator (D).

Interlock door contacts

The contractor must ensure that the interlock door contacts (B) are mounted as per the drawings and
cables are routed to the X-ray generator. It is allowed to use Philips dedicated cable ducting for this
purpose.
The Philips engineer will connect the cables to the X-ray generator (D).

Room emergency off switch

The contractor must ensure that the emergency off switch (C) is mounted as per the drawings and cables
are routed to the X-ray generator. It is allowed to use Philips dedicated cable ducting for this purpose.
The Philips engineer will connect the cables to the x-ray generator (D).
Room emergency off switch
The contractor must ensure that the emergency off switch (B) is mounted as per the drawings and cables
are routed to the Main cabinet. It is allowed to use Philips dedicated cable ducting for this purpose.
The Philips engineer will connect the cables to the Main cabinet (C).

3.2.7 Ducting specifications

The contractor must ensure that:
• Cable ducts and trays are routed as per the drawings.
• Upon completion of the Philips installation, all floor ducting must be suitably sealed to prevent
ingress fluids.
• All cable outlets are to be fitted with grommet strips to protect against chafing.
• All power cables are separated from any data cables within the ducting.
• All metal cable ducts are bonded and earthed according to local regulations.
The contractor must verify the feasibility of the cable routing as shown in the drawings, any changes should
be agreed with the Philips Healthcare project manager.
Chosen materials and methods must comply with local regulations and craftsmanship and prevent cable
bending radii smaller than 100 mm (unless specified otherwise).
The contractor must ensure that it is possible to access the ducting at any time during the life of the
equipment.
Where wiring is indicated point to point on the wiring diagram, it must be run in suitable ducting, cable
tray or conduit.

Electrical Page 14 of 21
3.4 Networking specifications
3.4.1 Local Area Network (LAN)
The contractor must ensure that the network connection points are supplied, fitted and connected as per
the drawings.
The contractor must work with the customer to ensure that a connection to the hospital network is
available, prior to the start of installation, at the network connection points as shown in the drawings.
The customer must allocate an IP address and other network specific information requested by Philips, for
each network connection shown in the drawings.
Further information and guidance on LAN setup and requirements will be provided by the Philips
Healthcare project manager.
3.4.2 Remote Service Network (RSN)
The system needs one or more Ethernet RJ-45 wall sockets with connection to the hospital network as per
the drawings. This connection needs to be setup according to the following specifications.
Important!
RSN Details
Please provide the Philips project manager in advance with the details.
• Full duplex network connection, 10BASE-T, 100BASE-T or 1000BASE-T
• Local f ixed IP address
• Corresponding subnet mask
• Corresponding gateway
• Minimum required speed: 128 Kbit/s

Electrical Page 15 of 21
4 Mechanical

4.1 General information

Please ensure that you read the other sections of this manual and take care to work with the other
contractors on any overlapping activity.
All work described must be carried out in compliance with specifications indicated in this package provided
by Philips Healthcare; any deviations must first be agreed by Philips Healthcare project manager.
All work described in this section is to be executed and supplied by the relevant contractor / party, unless
otherwise indicated as Philips Healthcare, or defined in a subsequent document

4.2 Heating, Ventilation & Air Conditioning (HVAC)

The Philips equipment requires the following temperature and humidity conditions:

Requirement Specification
Examination room
Temperature +18 to +30 °C
Relative humidity 30 - 75% (non-condensing)
Control room
Temperature +18 to +35 °C
Relative humidity 20 - 75% (non-condensing)
Technical room
Temperature +10 to +40 °C
Relative humidity 30 - 75% (non-condensing)

The following heat outputs of the Philips equipment must be taken into account, please refer to the
drawings for the precise locations.

(operational) (standby)
Ceiling suspension (CSV2) 425 (incl. tube) 50 (CSV2)
with longitudinal carriage
Patient table (DiDi TH 750mm) 150 (excl. detector) -
Vertical stand (VS2) wall mounted 180 130
X-ray generator (M-cabinet CXA Pro 50/65 kW) < 100 60
Eleva Workspot (AWS-TX + EEC-A) 230 (max) 20

4.3 Liquid cooling

The Philips equipment has no requirements in this discipline.

4.4 Water
The Philips equipment has no requirements in this discipline.

Mechanical Page 16 of 21
4.5 Sewerage
The Philips equipment has no requirements in this discipline.

4.6 Sprinkler
The Philips equipment has no requirements in this discipline.

4.7 Compressed air

The Philips equipment has no requirements in this discipline.

4.8 Gases
The Philips equipment has no requirements in this discipline.

Mechanical Page 17 of 21
5 Environmental protection

5.1 X-ray
5.1.1 X-ray energy
The local radiation protection authority can use the following data to determine the correct
protection requirements.

Parameter Specification
Tube current 1 - 900 mA
Tube voltage 40 - 150 kV
mAs product 0.5 - 850 mAs
Exposure time 1 ms - 6 s / 16 s
Exposure frequency ≤ 12 exp./s

Environmental protection Page 18 of 21

6 Drawings

6.1 Site specific drawings

The technical drawings created for this project are added behind this page as a set.
The set normally contains the following drawings(can vary depending on building works and system
configuration) :
• Site layout
• Schematic cross section(s)
• Floor provisions
• Ceiling provisions
• Wall provisions
• Details
Refer to the table of contents on the cover page of the drawing set for the actual contents.
Important!
Not for construction!
The provided drawings are the graphical part of the site preparation specifications and not int ended
for direct application as construction drawings. It is the responsibility of the customer or contractor to
check the local feasibility of the provided specifications and solutions before embedding them into the
actual construction drawings.
If the customer or contractor decides to use the Philips drawings unchanged, mark each printed or
digital copy of each drawing sheet clearly with the following statement:
"Approved for construction by<name ofauthorized engineer> on behalf of<contractor>"
completed with the date and signature of the authorized engineer.

Drawings Page 19 of 21
7 Annex

7.1 Electrical diagram (example)

Philips
Customer
PPCB
PCB

RCD2
F4

Spare
ECB
Incoming power

L1,L2,L3,N

RCD1

M-CXA Pro
Generator
cabinet
GS1

F3
K1

L3
F2

L2
L1
K1
F1
Electrical panel

PE

EPO

EPO
ON/OFF
pushbutton

Requirement Specification

Voltage 3x 400/440/460/480 V ±10%

Frequency 47 - 63 Hz
Mains switch (GS1) -
Fuse protection
F1 F2 F3 F4
6A 2A 35 A / 50 A, slow blow 16 A
Residual current device
RCD 1 RCD 2
63 A / 0.03 A; Type B 16 / 0.03 A

Annex Page 20 of 21
Colophon

Philips Healthcare
A business of Royal Philips N.V.
www.philips.com/healthcare
healthcare@ philips.com

Your project is executed by

Philips Medical Systems Nederland B.V.
Veenpluis 4-6
5684 PC, Best, The Netherlands

www.healthcare.philips.com/main/support/support-for-your-site/site-planning/index.wpd

© 2016 Koninklijke Philips N.V.

All rights are rese rved
This document was assembled specifically for the project mentioned on the front page and contains
configuration and site specific information. Do not use for any other purpose.

Published by Philips Healthcare – Commercial Operations

Page 21 of 21